FDA Device recall Z-0348-2020
Energy FX: a) original Aluminum (100-3A) b) sleek (adult and kid & pet) (100-3B)
- FDA Device
- Class II
- completed
- Published 2019-11-20
On 2019-11-20 the FDA classified a Class II recall of Energy FX: a) original Aluminum (100-3A) b) sleek (adult and kid & pet) (100-3B) by Basic Reset, citing FDA determined that marketing claims surrounding product rendered product a medical device which was adulterated and misbranded.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0348-2020 |
| Classification | Class II |
| Status | completed |
| Initiated | 2019-10-18 |
| Published | 2019-11-20 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Basic Reset |
| Distribution | PR |
Product
Energy FX: a) original Aluminum (100-3A) b) sleek (adult and kid & pet) (100-3B)
Reason
FDA determined that marketing claims surrounding product rendered product a medical device which was adulterated and misbranded.
Identifiers
| code_info | All product distributed between November 7, 2017 to September 4, 2019 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0348-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.